Canonical Allele Identifier: CA9725746
Gene: RSPO4 HGNC NCBI

Linked Data

dbSNP Id: rs752640647
gnomAD v2: 20-948658-T-A
gnomAD v4: 20-968015-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968015T>A , CM000682.2:g.968015T>A GRCh38
NC_000020.10:g.948658T>A , CM000682.1:g.948658T>A GRCh37
NC_000020.9:g.896658T>A NCBI36
NG_013043.1:g.39250A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.203A>T MANE Select ENSP00000217260.4:p.Lys68Met
ENST00000217260.8:c.203A>T ENSP00000217260.4:p.Lys68Met
ENST00000400634.2:c.203A>T ENSP00000383475.2:p.Lys68Met
NM_001029871.3:c.203A>T NP_001025042.2:p.Lys68Met
NM_001040007.2:c.203A>T NP_001035096.1:p.Lys68Met
XM_011529232.1:c.251A>T XP_011527534.1:p.Lys84Met
XM_011529233.1:c.251A>T XP_011527535.1:p.Lys84Met
XR_937068.1:n.323A>T
XR_937069.1:n.318A>T
XM_017027839.1:c.203A>T XP_016883328.1:p.Lys68Met
NM_001029871.4:c.203A>T MANE Select NP_001025042.2:p.Lys68Met
NM_001040007.3:c.203A>T NP_001035096.1:p.Lys68Met